Pradervand Nicolas, Delavat François, Sulser Sandra, Miyazaki Ryo, van der Meer Jan Roelof
Department of Fundamental Microbiology, University of Lausanne, Lausanne, Switzerland.
Department of Fundamental Microbiology, University of Lausanne, Lausanne, Switzerland
J Bacteriol. 2014 Nov;196(22):3971-9. doi: 10.1128/JB.02129-14. Epub 2014 Sep 2.
Integrative and conjugating elements (ICE) are self-transferable DNAs widely present in bacterial genomes, which often carry a variety of auxiliary genes of potential adaptive benefit. One of the model ICE is ICEclc, an element originally found in Pseudomonas knackmussii B13 and known for its propensity to provide its host with the capacity to metabolize chlorocatechols and 2-aminophenol. In this work, we studied the mechanism and target of regulation of MfsR, a TetR-type repressor previously found to exert global control on ICEclc horizontal transfer. By using a combination of ICEclc mutant and transcriptome analysis, gene reporter fusions, and DNA binding assays, we found that MfsR is a repressor of both its own expression and that of a gene cluster putatively coding for a major facilitator superfamily efflux system on ICEclc (named mfsABC). Phylogenetic analysis suggests that mfsR was originally located immediately adjacent to the efflux pump genes but became displaced from its original cis target DNA by a gene insertion. This resulted in divergence of the original bidirectional promoters into two separated individual regulatory units. Deletion of mfsABC did not result in a strong phenotype, and despite screening a large number of compounds and conditions, we were unable to define the precise current function or target of the putative efflux pump. Our data reconstruct how the separation of an ancestor mfsR-mfsABC system led to global control of ICEclc transfer by MfsR.
整合与接合元件(ICE)是广泛存在于细菌基因组中的可自我转移的DNA,其通常携带多种具有潜在适应性益处的辅助基因。ICEclc是一种典型的ICE,最初在克氏假单胞菌B13中发现,因其能够赋予宿主代谢氯儿茶酚和2-氨基酚的能力而闻名。在这项研究中,我们研究了MfsR的调控机制和靶点,MfsR是一种先前发现对ICEclc水平转移发挥全局控制作用的TetR型阻遏蛋白。通过结合ICEclc突变体和转录组分析、基因报告融合以及DNA结合试验,我们发现MfsR不仅抑制其自身的表达,还抑制ICEclc上一个推测编码主要易化子超家族外排系统的基因簇(命名为mfsABC)的表达。系统发育分析表明,mfsR最初紧邻外排泵基因,但由于基因插入而从其原始的顺式靶DNA上移位。这导致原始的双向启动子分化为两个独立的调控单元。mfsABC的缺失并未导致明显的表型,并且尽管筛选了大量化合物和条件,我们仍无法确定推测的外排泵的确切当前功能或靶点。我们的数据重建了祖先mfsR-mfsABC系统的分离如何导致MfsR对ICEclc转移的全局控制。